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首页> 外文期刊>Pediatrics international : >Diagnostic and therapeutic value of naloxone after intoxication with tramadol in a young girl.
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Diagnostic and therapeutic value of naloxone after intoxication with tramadol in a young girl.

机译:在一个年轻女孩中,曲马多中毒后纳洛酮的诊断和治疗价值。

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摘要

Tramadol therapy has gained wide popularity in the last few years, not only with regard to cancer patients on chronic pain therapy, but also in other acute or chronic pain problems. It is an atypical analgesic, which is contraindicated in infants below 1 year of age. Tramadol has a dual mechanism of analgesic action. It inhibits re-uptake of norepinephrine and serotonin, in addition to mu-opioid receptors agonism. The former action is mostly due to the parent compound tramadol, while its metabolite O-demethyltramadol (Ml) exerts its primary action at the mu-opioid receptor. Tramadol metabolite Ml is mainly formed by genetically polymorphic cytochrome P450 (CYP) 2D6. In extensive CYP2D6 metabolizers the analgesic effects of tramadol are superior to those in poor metabolizers.1 Unintentional intoxication with severe central nervous system (CNS) depression and seizures has been reported in small children. We report a case of tramadol intoxication in which treatment with naloxone was diagnostic and therapeutic.
机译:在过去的几年中,曲马多疗法不仅在接受慢性疼痛治疗的癌症患者中,而且在其他急性或慢性疼痛问题中,都得到了广泛的普及。这是一种非典型的止痛药,不适合1岁以下的婴儿使用。曲马多具有止痛作用的双重机理。除μ阿片受体激动剂外,它还抑制了去甲肾上腺素和5-羟色胺的再摄取。前一作用主要归因于母体化合物曲马多,而其代谢产物O-去甲基曲马多(M1)在μ阿片受体上发挥其主要作用。曲马多代谢物M1主要由基因多态性细胞色素P450(CYP)2D6形成。在广泛的CYP2D6代谢物中,曲马多的镇痛作用优于不良代谢者。1据报道,在幼儿中,无意中毒伴有严重的中枢神经系统(CNS)抑郁和癫痫发作。我们报告一例曲马多中毒事件,其中纳洛酮治疗具有诊断和治疗意义。

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